PL162983B1 - Srodek szkodnikobójczy PL PL - Google Patents

Srodek szkodnikobójczy PL PL

Info

Publication number: PL162983B1
Authority: PL; Poland
Prior art keywords: spp; dichloro; cyano; trifluoromethylphenyl; general formula
Prior art date: 1989-06-16

Application number

PL28564890A

Other languages

English (en)

Polish (pl)

Other versions

PL285648A1 (en

Inventor

David Alan Roberts

David William Hawkins

Ian George Buntain

Ross Mcguire

Original Assignee

Rhone Poulenc Agriculture

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1989-06-16

Filing date

1990-06-15

Publication date

1994-01-31

1990-06-15 Application filed by Rhone Poulenc Agriculture filed Critical Rhone Poulenc Agriculture

1991-02-25 Publication of PL285648A1 publication Critical patent/PL285648A1/xx

1994-01-31 Publication of PL162983B1 publication Critical patent/PL162983B1/pl

Links

239000000575 pesticide Substances 0.000 title claims description 3
125000005843 halogen group Chemical group 0.000 claims abstract description 10
125000000217 alkyl group Chemical group 0.000 claims abstract description 8
WITMXBRCQWOZPX-UHFFFAOYSA-N 1-phenylpyrazole Chemical class C1=CC=NN1C1=CC=CC=C1 WITMXBRCQWOZPX-UHFFFAOYSA-N 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 81
239000000203 mixture Substances 0.000 claims description 46
-1 2,6-dichloro-4-trifluoromethylphenyl amines Chemical class 0.000 claims description 28
239000003795 chemical substances by application Substances 0.000 claims description 26
125000004432 carbon atom Chemical group C* 0.000 claims description 7
229910052740 iodine Inorganic materials 0.000 claims description 6
239000002671 adjuvant Substances 0.000 claims description 3
239000011248 coating agent Substances 0.000 claims description 2
238000000576 coating method Methods 0.000 claims description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
125000004953 trihalomethyl group Chemical group 0.000 claims description 2
239000013543 active substance Substances 0.000 claims 2
AZVHKAHUXULCJJ-UHFFFAOYSA-N 1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-5-(trifluoromethylsulfanyl)-4-(trifluoromethylsulfonyl)pyrazole-3-carbonitrile Chemical compound FC(F)(F)SC1=C(S(=O)(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl AZVHKAHUXULCJJ-UHFFFAOYSA-N 0.000 claims 1
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229910052736 halogen Inorganic materials 0.000 abstract description 5
150000002367 halogens Chemical class 0.000 abstract description 3
108010034145 Helminth Proteins Proteins 0.000 abstract 1
125000003342 alkenyl group Chemical group 0.000 abstract 1
125000003545 alkoxy group Chemical group 0.000 abstract 1
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VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 57
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 38
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WQOXQRCZOLPYPM-UHFFFAOYSA-N dimethyl disulfide Chemical compound CSSC WQOXQRCZOLPYPM-UHFFFAOYSA-N 0.000 description 4
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CBFIKOBUXGUSNV-UHFFFAOYSA-N 5-bromo-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(trifluoromethylsulfonyl)pyrazole-3-carbonitrile Chemical compound ClC1=CC(C(F)(F)F)=CC(Cl)=C1N1C(Br)=C(S(=O)(=O)C(F)(F)F)C(C#N)=N1 CBFIKOBUXGUSNV-UHFFFAOYSA-N 0.000 description 3
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XQUXKZZNEFRCAW-UHFFFAOYSA-N fenpropathrin Chemical compound CC1(C)C(C)(C)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 XQUXKZZNEFRCAW-UHFFFAOYSA-N 0.000 description 1
YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 description 1
244000037666 field crops Species 0.000 description 1
FQXWEKADCSXYOC-UHFFFAOYSA-N fipronil-sulfide Chemical compound NC1=C(SC(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl FQXWEKADCSXYOC-UHFFFAOYSA-N 0.000 description 1
238000003818 flash chromatography Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
230000037406 food intake Effects 0.000 description 1
239000003205 fragrance Substances 0.000 description 1
230000000855 fungicidal effect Effects 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 1
JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
230000005484 gravity Effects 0.000 description 1
235000021384 green leafy vegetables Nutrition 0.000 description 1
210000004209 hair Anatomy 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
230000002458 infectious effect Effects 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 1
229960002809 lindane Drugs 0.000 description 1
241000238565 lobster Species 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
239000000391 magnesium silicate Substances 0.000 description 1
229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
229960000453 malathion Drugs 0.000 description 1
235000013372 meat Nutrition 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000000034 method Methods 0.000 description 1
UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 1
VYHVQEYOFIYNJP-UHFFFAOYSA-N methyl thiocyanate Chemical compound CSC#N VYHVQEYOFIYNJP-UHFFFAOYSA-N 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000013379 molasses Nutrition 0.000 description 1
KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 description 1
238000000465 moulding Methods 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012457 nonaqueous media Substances 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
244000045947 parasite Species 0.000 description 1
LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 description 1
229960000490 permethrin Drugs 0.000 description 1
RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000003016 pheromone Substances 0.000 description 1
IOUNQDKNJZEDEP-UHFFFAOYSA-N phosalone Chemical compound C1=C(Cl)C=C2OC(=O)N(CSP(=S)(OCC)OCC)C2=C1 IOUNQDKNJZEDEP-UHFFFAOYSA-N 0.000 description 1
229960005235 piperonyl butoxide Drugs 0.000 description 1
YFGYUFNIOHWBOB-UHFFFAOYSA-N pirimicarb Chemical compound CN(C)C(=O)OC1=NC(N(C)C)=NC(C)=C1C YFGYUFNIOHWBOB-UHFFFAOYSA-N 0.000 description 1
QHOQHJPRIBSPCY-UHFFFAOYSA-N pirimiphos-methyl Chemical group CCN(CC)C1=NC(C)=CC(OP(=S)(OC)OC)=N1 QHOQHJPRIBSPCY-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
244000144977 poultry Species 0.000 description 1
235000015136 pumpkin Nutrition 0.000 description 1
150000003217 pyrazoles Chemical class 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
239000005871 repellent Substances 0.000 description 1
230000002940 repellent Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
210000003491 skin Anatomy 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
239000004550 soluble concentrate Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000003892 spreading Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
235000013616 tea Nutrition 0.000 description 1
CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
235000019731 tricalcium phosphate Nutrition 0.000 description 1
229940096911 trichinella spiralis Drugs 0.000 description 1
125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
GRGCWBWNLSTIEN-UHFFFAOYSA-N trifluoromethanesulfonyl chloride Chemical compound FC(F)(F)S(Cl)(=O)=O GRGCWBWNLSTIEN-UHFFFAOYSA-N 0.000 description 1
239000002966 varnish Substances 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
230000003612 virological effect Effects 0.000 description 1
239000003643 water by type Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
239000000230 xanthan gum Substances 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1
229940082509 xanthan gum Drugs 0.000 description 1
235000010493 xanthan gum Nutrition 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/28—Two oxygen or sulfur atoms
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Wood Science & Technology (AREA)
Environmental Sciences (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Pest Control & Pesticides (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Soundproofing, Sound Blocking, And Sound Damping (AREA)
External Artificial Organs (AREA)
Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
Separation Of Suspended Particles By Flocculating Agents (AREA)
Fats And Perfumes (AREA)
Lubricants (AREA)
Compositions Of Macromolecular Compounds (AREA)

PL28564890A 1989-06-16 1990-06-15 Srodek szkodnikobójczy PL PL PL162983B1 (pl)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB898913888A GB8913888D0 (en)	1989-06-16	1989-06-16	New compositions of matter

Publications (2)

Publication Number	Publication Date
PL285648A1 PL285648A1 (en)	1991-02-25
PL162983B1 true PL162983B1 (pl)	1994-01-31

Family

ID=10658564

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PL28564890A PL162983B1 (pl)	1989-06-16	1990-06-15	Srodek szkodnikobójczy PL PL

Country Status (33)

Country	Link
EP (1)	EP0403309B1 (fr)
JP (1)	JP2963495B2 (fr)
KR (1)	KR0160769B1 (fr)
CN (1)	CN1031543C (fr)
AT (1)	ATE113584T1 (fr)
AU (1)	AU5713190A (fr)
BG (1)	BG51143A3 (fr)
BR (1)	BR9002938A (fr)
CA (1)	CA2018403C (fr)
DD (1)	DD298782A5 (fr)
DE (1)	DE69013766T2 (fr)
DK (1)	DK0403309T3 (fr)
ES (1)	ES2066132T3 (fr)
FI (1)	FI103339B (fr)
GB (1)	GB8913888D0 (fr)
HU (1)	HU205604B (fr)
IE (1)	IE66314B1 (fr)
IL (1)	IL94746A (fr)
MA (1)	MA21872A1 (fr)
NO (1)	NO902657L (fr)
NZ (1)	NZ234080A (fr)
OA (1)	OA09452A (fr)
PE (1)	PE27491A1 (fr)
PH (1)	PH26911A (fr)
PL (1)	PL162983B1 (fr)
PT (1)	PT94386B (fr)
RU (1)	RU2026291C1 (fr)
TN (1)	TNSN90083A1 (fr)
TR (1)	TR24646A (fr)
UY (1)	UY23088A1 (fr)
YU (1)	YU116890A (fr)
ZA (1)	ZA904362B (fr)
ZW (1)	ZW10290A1 (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9306184D0 (en) *	1993-03-25	1993-05-19	Zeneca Ltd	Heteroaromatic compounds
US5629335A (en) *	1995-04-07	1997-05-13	Rhone-Poulenc Inc.	Pesticidal 1-arylpyrazole-3-carboximidothioic acid esters
US6136983A (en) *	1995-06-05	2000-10-24	Rhone-Poulenc Agrochimie	Pesticidal sulfur compounds
US6060502A (en) *	1995-06-05	2000-05-09	Rhone-Poulenc Agrochimie	Pesticidal sulfur compounds
US6060495A (en) *	1995-06-05	2000-05-09	Rhone-Poulenc Agrochimie	Pesticidal sulfur compounds
US6350771B1 (en)	1996-12-24	2002-02-26	Rhone-Poulenc, Inc.	Pesticidal 1-arylpyrazoles
ZA9711534B (en)	1996-12-24	1998-06-24	Rhone Poulenc Agrochimie	Pesticidal 1-arylpyrazoles.
ZA981934B (en) *	1997-03-10	1999-09-06	Rhone Poulenc Agrochimie	Pesticidal 1-aryl-3-iminopyrazoles.
ZA981776B (en)	1997-03-10	1998-09-03	Rhone Poulenc Agrochimie	Pesticidal 1-arylpyrazoles
US5981565A (en)	1997-10-07	1999-11-09	Rhone-Poulenc Inc.	Pyrazole pesticides
US6107314A (en)	1997-10-07	2000-08-22	Rhone-Poulenc Inc.	Pesticides
RU2252012C1 (ru) *	2003-10-10	2005-05-20	Иванова Елена Борисовна	Инсектицидный гель-приманка

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3002413A1 (de) *	1980-01-24	1981-07-30	Hoechst Ag, 6000 Frankfurt	N,n-dialkyl-o-(pyrazol-5-yl)-carbaminsaeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide
DE3617554A1 (de) *	1986-05-24	1987-11-26	Bayer Ag	5-oxy(thio)-pyrazol-derivate

1989
- 1989-06-16 GB GB898913888A patent/GB8913888D0/en active Pending
1990
- 1990-06-06 IE IE202890A patent/IE66314B1/en not_active IP Right Cessation
- 1990-06-06 ZA ZA904362A patent/ZA904362B/xx unknown
- 1990-06-06 CA CA002018403A patent/CA2018403C/fr not_active Expired - Lifetime
- 1990-06-11 MA MA22140A patent/MA21872A1/fr unknown
- 1990-06-14 YU YU01168/90A patent/YU116890A/xx unknown
- 1990-06-14 ZW ZW102/90A patent/ZW10290A1/xx unknown
- 1990-06-14 NO NO90902657A patent/NO902657L/no unknown
- 1990-06-14 PE PE1990170794A patent/PE27491A1/es unknown
- 1990-06-14 DD DD90341678A patent/DD298782A5/de not_active IP Right Cessation
- 1990-06-14 AU AU57131/90A patent/AU5713190A/en not_active Abandoned
- 1990-06-14 UY UY23088A patent/UY23088A1/es not_active IP Right Cessation
- 1990-06-15 NZ NZ234080A patent/NZ234080A/en unknown
- 1990-06-15 PL PL28564890A patent/PL162983B1/pl unknown
- 1990-06-15 OA OA59807A patent/OA09452A/xx unknown
- 1990-06-15 PH PH40682A patent/PH26911A/en unknown
- 1990-06-15 PT PT94386A patent/PT94386B/pt not_active IP Right Cessation
- 1990-06-15 HU HU903879A patent/HU205604B/hu unknown
- 1990-06-15 JP JP2157388A patent/JP2963495B2/ja not_active Expired - Lifetime
- 1990-06-15 EP EP90306578A patent/EP0403309B1/fr not_active Expired - Lifetime
- 1990-06-15 RU SU904830283A patent/RU2026291C1/ru active
- 1990-06-15 AT AT90306578T patent/ATE113584T1/de not_active IP Right Cessation
- 1990-06-15 DK DK90306578.7T patent/DK0403309T3/da active
- 1990-06-15 BG BG092236A patent/BG51143A3/bg unknown
- 1990-06-15 ES ES90306578T patent/ES2066132T3/es not_active Expired - Lifetime
- 1990-06-15 DE DE69013766T patent/DE69013766T2/de not_active Expired - Lifetime
- 1990-06-15 FI FI903037A patent/FI103339B/fi active IP Right Grant
- 1990-06-15 IL IL9474690A patent/IL94746A/en unknown
- 1990-06-15 TN TNTNSN90083A patent/TNSN90083A1/fr unknown
- 1990-06-16 KR KR1019900008879A patent/KR0160769B1/ko not_active Expired - Lifetime
- 1990-06-16 CN CN90103007A patent/CN1031543C/zh not_active Expired - Lifetime
- 1990-06-18 BR BR909002938A patent/BR9002938A/pt not_active IP Right Cessation
- 1990-06-18 TR TR90/0588A patent/TR24646A/xx unknown

Also Published As

Publication number	Publication date
DE69013766D1 (de)	1994-12-08
OA09452A (en)	1992-10-15
PE27491A1 (es)	1991-10-21
CN1031543C (zh)	1996-04-17
PH26911A (en)	1992-12-03
IE902028A1 (en)	1991-01-02
JP2963495B2 (ja)	1999-10-18
CA2018403A1 (fr)	1990-12-16
PL285648A1 (en)	1991-02-25
UY23088A1 (es)	1990-11-14
MA21872A1 (fr)	1990-12-31
KR0160769B1 (ko)	1998-12-01
DD298782A5 (de)	1992-03-12
RU2026291C1 (ru)	1995-01-09
ATE113584T1 (de)	1994-11-15
FI103339B1 (fi)	1999-06-15
IL94746A (en)	1995-03-30
IE66314B1 (en)	1995-12-27
JPH03109376A (ja)	1991-05-09
GB8913888D0 (en)	1989-08-02
DK0403309T3 (da)	1994-11-21
NZ234080A (en)	1991-04-26
ZW10290A1 (en)	1991-01-23
HUT54997A (en)	1991-04-29
BR9002938A (pt)	1991-11-12
NO902657L (no)	1990-12-17
FI103339B (fi)	1999-06-15
ES2066132T3 (es)	1995-03-01
EP0403309A1 (fr)	1990-12-19
YU116890A (en)	1991-10-31
PT94386A (pt)	1991-02-08
TR24646A (tr)	1992-01-01
BG51143A3 (bg)	1993-02-26
CA2018403C (fr)	2000-08-22
AU5713190A (en)	1990-12-20
HU903879D0 (en)	1990-11-28
IE902028L (en)	1990-12-16
ZA904362B (en)	1991-04-24
CN1048035A (zh)	1990-12-26
KR910000656A (ko)	1991-01-29
DE69013766T2 (de)	1995-04-06
FI903037A0 (fi)	1990-06-15
PT94386B (pt)	1996-12-31
TNSN90083A1 (fr)	1991-03-05
NO902657D0 (no)	1990-06-14
IL94746A0 (en)	1991-04-15
EP0403309B1 (fr)	1994-11-02
HU205604B (en)	1992-05-28

Publication	Publication Date	Title
JP2931046B2 (ja)	1999-08-09	Ｎ―フェニルピラゾール誘導体
FI100329B (fi)	1997-11-14	N-fenyylipyratsolijohdannaiset
AU653722B2 (en)	1994-10-13	Pesticidal 1-arylpyrroles
FI103338B (fi)	1999-06-15	Pestisidinä käytettävät N-fenyylipyratsolijohdannaiset
EP0372982B1 (fr)	1997-07-02	Insecticides contenant des pyrroles
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